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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388177Generated: November 3, 2026

Benzoyl chloride, 3,4-dichloro- → 3,4-Dichloro-N-(1-methyl-1-azaspiro[4.5]decan-4-yl)benzamide

https://huagongshe.com/reaction/1388177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 70447095HCID 70447095—
SolventChloroformHCID 6212—
Product3,4-Dichloro-N-(1-methyl-1-azaspiro[4.5]decan-4-yl)benzamideHCID 1328285644.8%

Reaction Steps

To a stirring suspension of 3.0 g (0.017 mole) of 1-methyl-4-amino-1-azaspiro[4.5]decane of Example 2 and 5.0 g of NaHCO3 in 50 ml of CHCl3 was added dropwise 3.8 g (0.018 mole) of 3,4-dichlorobenzoyl chloride in 25 ml of CHCl3. The reaction was refluxed for 3 hours, cooled to room temperature, filtered, and the solvent evaporated to give an oil. The residue was triturated with boiling hexane and decanted, the hexane solution afforded 2.6 g of 1-methyl-4-(3,4-dichlorobenzamido)-1-azaspiro[4.5]decane on standing. The solid was dissolved in ether and a solution of ethereal HCl was added. The resulting solid was collected and recrystallized three times from ethanol to give 2.2 g (35%) m.p. 227°-228° C. of 1-methyl-4-(3,4-dichlorobenzamido)-1-azaspiro[4.5]decane hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04430335
Source datasetuspto-grants-1984_02
ORD IDord-fd10661e97c14113882eba753aea5cfa
Source noteuspto-grants-1984_02